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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047949Generated: October 30, 2026

Potassium Hydroxide → N-((6-(5-(But-3-enyloxy)-2,4-dimethylphenyl)pyridin-2-yl)methylene)-2,6-diisopropylaniline

https://huagongshe.com/reaction/2047949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant5-(But-3-enyloxy)-2,4-dimethylphenylboronic acidHCID 59479612—
ReactantN-[(6-Bromo-2-pyridinyl)methylene]-2,6-bis(1-methylethyl)benzenamineHCID 59479616—
CatalystHCID 178454878HCID 178454878—
SolventTetrahydrofuranHCID 8028—
ProductN-((6-(5-(But-3-enyloxy)-2,4-dimethylphenyl)pyridin-2-yl)methylene)-2,6-diisopropylanilineHCID 59479617—

Reaction Steps

In the glovebox, N-((6-bromopyridin-2-yl)methylene)-2,6-diisopropylaniline (1.392 g, 4.03 mmol) is combined with 5-(but-3-enyloxy)-2,4-dimethylphenylboronic acid (1.000 g, 4.03 mmol) and KOH (0.678 g, 12.1 mmol) and dry THF (40 mL) is added. Palladium(I) tri-tert-butylphosphine bromide, dimer [PtBu3)PdBr]2 (0.062 g, 0.040 mmol) is added and the reaction mixture is stirred for five hours, removed from the glovebox, and ether (100 mL) is added. The solution is washed with water (50 mL) and then brine (50 mL), dried over magnesium sulfate, filtered, and solvents removed by evaporation. Yield=1.86 g of orange sticky oil. The product is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592615B2
Source datasetuspto-grants-2013_11
ORD IDord-8a50c24fee944aaf8504f487d0ca5fe4
Source noteuspto-grants-2013_11